Experience

Clinscience

• Poland
• Research Services
• 100 - 200 Employee

• Clinical Research Associate (CRA) Trainee

  • Jan 2023 - Present

  Conducting initiation, monitoring and closure visits of Phase I-III clinical trialssupporting sites to adapt and drive recruitment plans. Collaboration with investigators, SC and other site personnel providingtraining and ensuring proper trial conduct. Maintenance of appropriate site documentation. Review and verification of clinical data collected ensuring accuracy,completeness and protocol compliance. Identifying and resolving any problems or deviations from the protocol. Conducting initiation, monitoring and closure visits of Phase I-III clinical trialssupporting sites to adapt and drive recruitment plans. Collaboration with investigators, SC and other site personnel providingtraining and ensuring proper trial conduct. Maintenance of appropriate site documentation. Review and verification of clinical data collected ensuring accuracy,completeness and protocol compliance. Identifying and resolving any problems or deviations from the protocol.



Instituto Bernabeu

• Spain
• Hospitals and Health Care
• 100 - 200 Employee

• Embrióloga

  • Aug 2015 - Present

  Drafting of protocols for presentation to the drug research ethics committee. Trial coordination: management of the process of obtaining informed consent.Recording of clinical data obtained in the patient's clinical history and in thedata collection notebook. Management and maintenance of the necessarytrial documentation. Teaching in embryo biopsy workshops at blastocyst stage. Semen sample processing and technical control of the laboratory. In vitro fertilization (classical and ICSI). Vitrification/devitrification of oocytes and embryos. Classification and embryo transfer. Embryo biopsy at blastocyst stage. Show less